Mucinex Sinus - Max
- Product NDC
- 63824-690
- 11-digit product format
- 638240690
- Labeler code
- 63824
- Product ID
- 63824-690_eb53cf21-3159-43be-e053-2995a90ab63d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Guaifenesin, Phenylephrine hydrochloride
- Dosage form
- KIT
- Labeler
- RB Health (US) LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-07-15
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63824-690-24 | 63824069024 | 1 KIT in 1 CARTON (63824-690-24) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2015-07-15 | 0000-00-00 | No | No | Current |
| 63824-690-48 | 63824069048 | 1 KIT in 1 CARTON (63824-690-48) * 4 BLISTER PACK in 1 CARTON > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2015-07-15 | 0000-00-00 | No | No | Current |